VANGUARD REPROCESSED PULSE OXIMETER SENSORS— 510(k) K042316
Substantially EquivalentVanguard Medical Concepts, Inc.
FDA 510(k) clearance K042316 for VANGUARD REPROCESSED PULSE OXIMETER SENSORS, Substantially Equivalent on 2005-01-06. Applicant: Vanguard Medical Concepts, Inc.. Device class: 2.
Clearance details
- Applicant
- Vanguard Medical Concepts, Inc.
- Product code
- Code NLF
- Device class
- Class 2
- Regulation
- 21 CFR 870.2700
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lakeland, FL, US
Recent devices under product code NLF
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More clearances from Vanguard Medical Concepts, Inc.
view all- K053051 — VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES
- K051616 — VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES
- K051180 — VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES
- K051043 — VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS
- K050763 — VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS
Data sourced from openFDA. This site is unofficial and independent of the FDA.